NDC Package 24571-113-06 Prismasol Bk0/0/1.2

Magnesium Chloride,Lactic Acid,Sodium Chloride And Sodium Bicarbonate Injection - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
24571-113-06
Package Description:
2 BAG in 1 CASE / 5 L in 1 BAG
Product Code:
Proprietary Name:
Prismasol Bk0/0/1.2
Non-Proprietary Name:
Magnesium Chloride, Lactic Acid, Sodium Chloride And Sodium Bicarbonate
Substance Name:
Lactic Acid, Unspecified Form; Magnesium Chloride; Sodium Bicarbonate; Sodium Chloride
Usage Information:
PRISMASOL and PHOXILLUM solutions are indicated in pediatric and adult patients for use as a replacement solution in Continuous Renal Replacement Therapy (CRRT) to replace plasma volume removed by ultrafiltration and to correct electrolyte and acid-base imbalances. They may also be used in case of drug poisoning when CRRT is used to remove dialyzable substances.
11-Digit NDC Billing Format:
24571011306
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
5000 ML
Product Type:
Human Prescription Drug
Labeler Name:
Baxter Healthcare Corporation
Dosage Form:
Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Sample Package:
    No
    FDA Application Number:
    NDA021703
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    10-25-2006
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 24571-113-06?

    The NDC Packaged Code 24571-113-06 is assigned to a package of 2 bag in 1 case / 5 l in 1 bag of Prismasol Bk0/0/1.2, a human prescription drug labeled by Baxter Healthcare Corporation. The product's dosage form is injection and is administered via intravenous form.This product is billed per "ML" milliliter and contains an estimated amount of 5000 billable units per package.

    Is NDC 24571-113 included in the NDC Directory?

    Yes, Prismasol Bk0/0/1.2 with product code 24571-113 is active and included in the NDC Directory. The product was first marketed by Baxter Healthcare Corporation on October 25, 2006 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 24571-113-06?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 5000.

    What is the 11-digit format for NDC 24571-113-06?

    The 11-digit format is 24571011306. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-224571-113-065-4-224571-0113-06